Interdisciplinary Scientist Training Program, University of Chicago, Chicago, IL, USA.
Committee on Immunology, University of Chicago, Chicago, IL, USA.
Nat Immunol. 2023 Mar;24(3):487-500. doi: 10.1038/s41590-023-01425-0. Epub 2023 Feb 9.
The T cell repertoire of healthy mice and humans harbors self-reactive CD4 conventional T (T) cells capable of inducing autoimmunity. Using T cell receptor profiling paired with in vivo clonal analysis of T cell differentiation, we identified T cell clones that are recurrently enriched in non-lymphoid organs following ablation of Foxp3 regulatory T (T) cells. A subset of these clones was highly proliferative in the lymphoid organs at steady state and exhibited overt reactivity to self-ligands displayed by dendritic cells, yet were not purged by clonal deletion. These clones spontaneously adopted numerous hallmarks of follicular helper T (T) cells, including expression of Bcl6 and PD-1, exhibited an elevated propensity to localize within B cell follicles at steady state, and produced interferon-γ in non-lymphoid organs following sustained T cell depletion. Our work identifies a naturally occurring population of self-reactive T-like cells and delineates a previously unappreciated fate for self-specific T cells.
健康小鼠和人类的 T 细胞库中存在自身反应性 CD4 常规 T(T)细胞,这些细胞能够引发自身免疫。我们使用 T 细胞受体谱分析并结合 T 细胞分化的体内克隆分析,鉴定出在 Foxp3 调节性 T(T)细胞耗竭后,经常在非淋巴器官中富集的 T 细胞克隆。这些克隆中的一部分在稳定状态下在淋巴器官中具有高度增殖性,并表现出对树突状细胞表面自身配体的明显反应性,但未被克隆删除清除。这些克隆自发地采用了滤泡辅助 T(T)细胞的许多特征,包括表达 Bcl6 和 PD-1,在稳定状态下具有更高的倾向定位于 B 细胞滤泡内,并在持续 T 细胞耗竭后在非淋巴器官中产生干扰素-γ。我们的工作鉴定了一种自然发生的自身反应性 T 样细胞群体,并描绘了以前未被重视的自身特异性 T 细胞命运。